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Showing articles 0 to 6 of 6 Filter Applied: cerebrovascular accident,familial occurrence (Click to remove) Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients Neurol 74:57-63, Pantoni,L.,et al, 2010 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia Stroke 32:877-882, Maher,C.O.,et al, 2001 Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 Clinical Spectrum of CADASIL:A Study of 7 Families Lancet 346:934-939, Chabriat,H.,et al, 1995 Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage Lancet 2:603-604, Palsdottir,A.,et al, 1988 Showing articles 0 to 6 of 6